Have myositis questions for a rheumatologist? Now's your chance to get expert insight in a relaxed, open format. Join us for a special Ask the Expert session featuring Christopher Mecoli, MD, MHS, Associate Professor of Medicine; Director of Research Operations and Physician Lead for the Myositis Precision Center of Excellence at Johns Hopkins University. Dr. Christopher...
Every day, individuals living with myositis face muscle weakness, fatigue, isolation, and uncertainty. But they don’t have to face it alone. Through education, support groups, research funding, and advocacy, The Myositis Association (TMA) connects patients and families to the resources and community they need to move forward with strength and hope. Your gift fuels critical...
May is Myositis Awareness Month! It’s a time for the myositis community to raise our collective voices and let the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources and education, sharing strategies for advocacy, and building...
Save the Date! MyoCon: TMA's Global Myositis Patient Conference September 16–19, 2026 Marriott Marquis | Atlanta, GA TMA's 2027 Global Patient Conference will take place in Atlanta, Georgia on September 16–19. MyoCon is a cornerstone of TMA's patient education, engagement, connection, and support - a celebration you don't want to miss!
May is Myositis Awareness Month! It’s a time for the myositis community to raise our collective voices and let the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources and education, sharing strategies for advocacy, and building...
Save the Date! MyoCon: TMA's Global Myositis Patient Conference September 14–17, 2026 Westin| Lake Las Vegas, NV TMA's 2028 Global Patient Conference will take place in Lake Las Vegas, Nevada on September 14–17. MyoCon is a cornerstone of TMA's patient education, engagement, connection, and support - a celebration you don't want to miss!
May is Myositis Awareness Month! It’s a time for the myositis community to raise our collective voices and let the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources and education, sharing strategies for advocacy, and building...
May is Myositis Awareness Month! It’s a time for the myositis community to raise our collective voices and let the world know what this rare disease is all about. It’s TMA’s mission to support those who live with myositis and their care partners by bringing awareness, sharing resources and education, sharing strategies for advocacy, and building...